Canonical Allele Identifier: CA463850500
Gene: DMRT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.841904A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.841904A>C , CM000671.2:g.841904A>C GRCh38
NC_000009.11:g.841904A>C , CM000671.1:g.841904A>C GRCh37
NC_000009.10:g.831904A>C NCBI36
NG_009221.1:g.5215A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382276.8:c.66A>C MANE Select ENSP00000371711.3:p.Val22=
ENST00000382276.7:c.66A>C ENSP00000371711.3:p.Val22=
ENST00000564322.1:n.215A>C
NM_021951.2:c.66A>C NP_068770.2:p.Val22=
XM_006716732.1:c.66A>C XP_006716795.1:p.Val22=
XM_017014375.1:c.66A>C XP_016869864.1:p.Val22=
NM_021951.3:c.66A>C MANE Select NP_068770.2:p.Val22=