Linked Data
dbSNP Id:
rs536267051
gnomAD v2:
6-32149745-G-A
gnomAD v3:
6-32181968-G-A
gnomAD v4:
6-32181968-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32181968G>A , CM000668.2:g.32181968G>A | GRCh38 |
| NC_000006.11:g.32149745G>A , CM000668.1:g.32149745G>A | GRCh37 |
| NC_000006.10:g.32257723G>A | NCBI36 |
| NG_029868.1:g.7355C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375076.9:c.964+279C>T MANE Select | ENSP00000364217.4:n.964+279C>T | |
| ENST00000375055.6:c.964+279C>T | ENSP00000364195.2:n.964+279C>T | |
| ENST00000375065.6:c.151+279C>T | ENSP00000364206.6:n.151+279C>T | |
| ENST00000375067.7:c.810-336C>T | ENSP00000364208.3:n.810-336C>T | |
| ENST00000375069.7:c.1012+279C>T | ENSP00000364210.4:n.1012+279C>T | |
| ENST00000375070.7:c.661+279C>T | ENSP00000364211.4:n.661+279C>T | |
| ENST00000375076.8:c.964+279C>T | ENSP00000364217.4:n.964+279C>T | |
| ENST00000438221.6:c.1012+279C>T | ENSP00000387887.2:n.1012+279C>T | |
| ENST00000473619.5:n.506+279C>T | ||
| ENST00000484849.5:n.1171+279C>T | ||
| ENST00000488669.5:n.506+279C>T | ||
| ENST00000620802.4:c.283-535C>T | ENSP00000484081.1:n.283-535C>T | |
| NM_001136.4:c.964+279C>T | NP_001127.1:n.964+279C>T | |
| NM_001206929.1:c.1012+279C>T | NP_001193858.1:n.1012+279C>T | |
| NM_001206932.1:c.922+279C>T | NP_001193861.1:n.922+279C>T | |
| NM_001206934.1:c.1012+279C>T | NP_001193863.1:n.1012+279C>T | |
| NM_001206936.1:c.912+279C>T | NP_001193865.1:n.912+279C>T | |
| NM_001206940.1:c.964+279C>T | NP_001193869.1:n.964+279C>T | |
| NM_001206954.1:c.823-336C>T | NP_001193883.1:n.823-336C>T | |
| NM_001206966.1:c.964+279C>T | NP_001193895.1:n.964+279C>T | |
| NM_172197.2:c.810-336C>T | NP_751947.1:n.810-336C>T | |
| NR_038190.1:n.1247+279C>T | ||
| XM_017010328.2:c.964-336C>T | XP_016865817.1:n.964-336C>T | |
| XR_001743189.2:n.1029-336C>T | ||
| XR_001743190.2:n.981-336C>T | ||
| NM_001136.5:c.964+279C>T MANE Select | NP_001127.1:n.964+279C>T | |
| NM_001206932.2:c.922+279C>T | NP_001193861.1:n.922+279C>T | |
| NM_001206936.2:c.912+279C>T | NP_001193865.1:n.912+279C>T | |
| NM_001206940.2:c.964+279C>T | NP_001193869.1:n.964+279C>T | |
| NM_001206954.2:c.823-336C>T | NP_001193883.1:n.823-336C>T | |
| NM_001206966.2:c.964+279C>T | NP_001193895.1:n.964+279C>T | |
| NM_172197.3:c.810-336C>T | NP_751947.1:n.810-336C>T | |
| NR_038190.2:n.1178+279C>T | ||
| NM_001206929.2:c.1012+279C>T | NP_001193858.1:n.1012+279C>T | |
| NM_001206934.2:c.1012+279C>T | NP_001193863.1:n.1012+279C>T |