Linked Data
dbSNP Id:
rs753876731
ExAC:
2:215845303 G / C
gnomAD v2:
2-215845303-G-C
gnomAD v4:
2-214980579-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214980579G>C , CM000664.2:g.214980579G>C | GRCh38 |
| NC_000002.11:g.215845303G>C , CM000664.1:g.215845303G>C | GRCh37 |
| NC_000002.10:g.215553548G>C | NCBI36 |
| NG_007074.1:g.162849C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272895.12:c.4644C>G MANE Select | ENSP00000272895.7:p.Ala1548= | |
| ENST00000272895.11:c.4644C>G | ENSP00000272895.7:p.Ala1548= | |
| ENST00000389661.4:c.3690C>G | ENSP00000374312.4:p.Ala1230= | |
| NM_015657.3:c.3690C>G | NP_056472.2:p.Ala1230= | |
| NM_173076.2:c.4644C>G | NP_775099.2:p.Ala1548= | |
| NR_103740.1:n.4944C>G | ||
| XM_011510951.1:c.4653C>G | XP_011509253.1:p.Ala1551= | |
| XM_011510952.1:c.4653C>G | XP_011509254.1:p.Ala1551= | |
| XM_011510951.2:c.4653C>G | XP_011509253.1:p.Ala1551= | |
| NM_173076.3:c.4644C>G MANE Select | NP_775099.2:p.Ala1548= | |
| NR_103740.2:n.5142C>G | ||
| NM_015657.4:c.3690C>G | NP_056472.2:p.Ala1230= |