Linked Data
dbSNP Id:
rs777960396
gnomAD v2:
5-134366775-G-A
gnomAD v3:
5-135031085-G-A
gnomAD v4:
5-135031085-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135031085G>A , CM000667.2:g.135031085G>A | GRCh38 |
| NC_000005.9:g.134366775G>A , CM000667.1:g.134366775G>A | GRCh37 |
| NC_000005.8:g.134394674G>A | NCBI36 |
| NG_012114.1:g.8190C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.402+191C>T MANE Select | ENSP00000265340.6:n.402+191C>T | |
| ENST00000265340.11:c.402+191C>T | ENSP00000265340.6:n.402+191C>T | |
| ENST00000503586.1:c.524+191C>T | ||
| ENST00000504936.1:n.735+191C>T | ||
| ENST00000506438.5:c.402+191C>T | ENSP00000427542.1:n.402+191C>T | |
| NM_002653.4:c.402+191C>T | NP_002644.4:n.402+191C>T | |
| NM_002653.5:c.402+191C>T MANE Select | NP_002644.4:n.402+191C>T |