Linked Data
dbSNP Id:
rs1065386
gnomAD v2:
6-31324547-G-A
gnomAD v3:
6-31356770-G-A
gnomAD v4:
6-31356770-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31356770G>A , CM000668.2:g.31356770G>A | GRCh38 |
| NC_000006.11:g.31324547G>A , CM000668.1:g.31324547G>A | GRCh37 |
| NC_000006.10:g.31432526G>A | NCBI36 |
| NG_023187.1:g.5443C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.1734C>T | ||
| ENST00000481849.6:n.1734C>T | ||
| ENST00000497377.6:n.1734C>T | ||
| ENST00000640094.2:c.261C>T | ENSP00000491275.2:p.Asn87= | |
| ENST00000696558.1:c.261C>T | ENSP00000512716.1:p.Asn87= | |
| ENST00000696559.1:c.261C>T | ENSP00000512717.1:p.Asn87= | |
| ENST00000696560.1:c.261C>T | ENSP00000512718.1:p.Asn87= | |
| ENST00000696561.1:c.261C>T | ENSP00000512719.1:p.Asn87= | |
| ENST00000696562.1:c.261C>T | ENSP00000512720.1:p.Asn87= | |
| ENST00000412585.7:c.261C>T MANE Select | ENSP00000399168.2:p.Asn87= | |
| ENST00000412585.6:c.261C>T | ENSP00000399168.2:p.Asn87= | |
| ENST00000434333.1:c.294C>T | ENSP00000405931.1:p.Asn98= | |
| ENST00000474381.1:n.136C>T | ||
| ENST00000498007.1:n.282C>T | ||
| ENST00000603274.1:n.124G>A | ||
| NM_005514.6:c.261C>T | NP_005505.2:p.Asn87= | |
| XM_011514556.1:c.294C>T | XP_011512858.1:p.Asn98= | |
| XM_011514557.1:c.261C>T | XP_011512859.1:p.Asn87= | |
| XR_926175.1:n.271C>T | ||
| NM_005514.7:c.261C>T | NP_005505.2:p.Asn87= | |
| NM_005514.8:c.261C>T MANE Select | NP_005505.2:p.Asn87= |