Canonical Allele Identifier: CA396768436

Gene: FA2H

Linked Data

• gnomAD v4: 16-74774665-C-A
• MyVariant Identifiers: chr16:g.74808563C>A (hg19) ; chr16:g.74774665C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74774665C>A , CM000678.2:g.74774665C>A	GRCh38
NC_000016.9:g.74808563C>A , CM000678.1:g.74808563C>A	GRCh37
NC_000016.8:g.73366064C>A	NCBI36
NG_017070.1:g.5167G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000219368.8:c.91G>T MANE Select	ENSP00000219368.3:p.Ala31Ser
ENST00000219368.7:c.91G>T	ENSP00000219368.3:p.Ala31Ser
ENST00000567683.5:c.91G>T	ENSP00000455126.1:p.Ala31Ser
NM_024306.4:c.91G>T	NP_077282.3:p.Ala31Ser
XM_011523317.1:c.91G>T	XP_011521619.1:p.Ala31Ser
XM_011523318.1:c.91G>T	XP_011521620.1:p.Ala31Ser
XM_011523317.3:c.91G>T	XP_011521619.1:p.Ala31Ser
NM_024306.5:c.91G>T MANE Select	NP_077282.3:p.Ala31Ser