Linked Data
dbSNP Id:
rs782076049
ExAC:
11:70319329 G / T
gnomAD v2:
11-70319329-G-T
gnomAD v3:
11-70473224-G-T
gnomAD v4:
11-70473224-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.70473224G>T , CM000673.2:g.70473224G>T | GRCh38 |
| NC_000011.9:g.70319329G>T , CM000673.1:g.70319329G>T | GRCh37 |
| NC_000011.8:g.69996977G>T | NCBI36 |
| NG_042866.1:g.656573C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338508.9:c.3428C>A | ENSP00000345193.7:p.Ser1143Tyr | |
| ENST00000412252.6:c.973C>A | ENSP00000414876.2:n.973C>A | |
| ENST00000601538.6:c.5195C>A MANE Select | ENSP00000469689.2:p.Ser1732Tyr | |
| ENST00000654939.1:c.2704C>A | ||
| ENST00000656230.1:c.4058C>A | ENSP00000499561.1:p.Ser1353Tyr | |
| ENST00000659264.1:c.3485C>A | ENSP00000499270.1:p.Ser1162Tyr | |
| ENST00000338508.8:c.3431C>A | ENSP00000345193.6:p.Ser1144Tyr | |
| ENST00000357171.7:c.*199C>A | ENSP00000349694.4:n.*199C>A | |
| ENST00000409161.5:c.3407C>A | ENSP00000386491.1:p.Ser1136Tyr | |
| ENST00000412252.5:c.971C>A | ||
| ENST00000423696.6:c.4058C>A | ENSP00000394536.2:p.Ser1353Tyr | |
| ENST00000424924.5:c.3032C>A | ENSP00000402944.1:p.Ser1011Tyr | |
| ENST00000449833.6:c.3431C>A | ENSP00000399423.3:p.Ser1144Tyr | |
| ENST00000601538.5:c.5195C>A | ENSP00000469689.2:p.Ser1732Tyr | |
| ENST00000606715.3:n.1947C>A | ||
| NM_012309.4:c.5195C>A | NP_036441.2:p.Ser1732Tyr | |
| NM_133266.4:c.3431C>A | NP_573573.2:p.Ser1144Tyr | |
| NR_110766.1:n.1049C>A | ||
| XM_005277930.2:c.5195C>A | XP_005277987.1:p.Ser1732Tyr | |
| XM_005277932.2:c.4058C>A | XP_005277989.1:p.Ser1353Tyr | |
| XM_006718478.2:c.5165C>A | XP_006718541.1:p.Ser1722Tyr | |
| XM_011544854.1:c.5207C>A | XP_011543156.1:p.Ser1736Tyr | |
| XM_011544855.1:c.5186C>A | XP_011543157.1:p.Ser1729Tyr | |
| XM_011544856.1:c.5180C>A | XP_011543158.1:p.Ser1727Tyr | |
| XM_011544857.1:c.5159C>A | XP_011543159.1:p.Ser1720Tyr | |
| XM_011544859.1:c.4070C>A | XP_011543161.1:p.Ser1357Tyr | |
| XM_005277932.3:c.4058C>A | XP_005277989.1:p.Ser1353Tyr | |
| XM_017017387.1:c.5195C>A | XP_016872876.1:p.Ser1732Tyr | |
| XM_017017388.1:c.5195C>A | XP_016872877.1:p.Ser1732Tyr | |
| XM_017017389.1:c.5168C>A | XP_016872878.1:p.Ser1723Tyr | |
| XM_017017390.1:c.3485C>A | XP_016872879.1:p.Ser1162Tyr | |
| NM_133266.5:c.3431C>A | NP_573573.2:p.Ser1144Tyr | |
| NR_110766.2:n.1050C>A | ||
| NM_001379226.1:c.4058C>A | NP_001366155.1:p.Ser1353Tyr | |
| NM_012309.5:c.5195C>A MANE Select | NP_036441.2:p.Ser1732Tyr |