Canonical Allele Identifier: CA496544006
Gene: FA2H HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.74750465G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74716567G>T , CM000678.2:g.74716567G>T GRCh38
NC_000016.9:g.74750465G>T , CM000678.1:g.74750465G>T GRCh37
NC_000016.8:g.73307966G>T NCBI36
NG_017070.1:g.63265C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.819C>A MANE Select ENSP00000219368.3:p.Pro273=
ENST00000219368.7:c.819C>A ENSP00000219368.3:p.Pro273=
ENST00000562145.1:n.540C>A
ENST00000567683.5:c.*98C>A ENSP00000455126.1:n.*98C>A
NM_024306.4:c.819C>A NP_077282.3:p.Pro273=
XM_011523319.1:c.579C>A XP_011521621.1:p.Pro193=
XM_011523317.3:c.*1683C>A XP_011521619.1:n.*1683C>A
XM_011523319.2:c.579C>A XP_011521621.1:p.Pro193=
NM_024306.5:c.819C>A MANE Select NP_077282.3:p.Pro273=