Canonical Allele Identifier: CA1642283
Gene: SIX3 HGNC NCBI

Linked Data

dbSNP Id: rs752797098
gnomAD v2: 2-45169434-G-A
gnomAD v4: 2-44942295-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942295G>A , CM000664.2:g.44942295G>A GRCh38
NC_000002.11:g.45169434G>A , CM000664.1:g.45169434G>A GRCh37
NC_000002.10:g.45022938G>A NCBI36
NG_016222.1:g.5398G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.191G>A MANE Select ENSP00000260653.3:p.Gly64Asp
ENST00000260653.4:c.191G>A ENSP00000260653.3:p.Gly64Asp
NM_005413.3:c.191G>A NP_005404.1:p.Gly64Asp
XM_011533042.1:c.191G>A XP_011531344.1:p.Gly64Asp
NM_005413.4:c.191G>A MANE Select NP_005404.1:p.Gly64Asp