Canonical Allele Identifier: CA2232921811
Gene: FA2H HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74713303A= , CM000678.2:g.74713303A= GRCh38
NC_000016.9:g.74747201A= , CM000678.1:g.74747201A= GRCh37
NC_000016.8:g.73304702A= NCBI36
NG_017070.1:g.66529T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.*887T= MANE Select ENSP00000219368.3:n.*887T=
ENST00000219368.7:c.*887T= ENSP00000219368.3:n.*887T=
ENST00000562145.1:n.1727T=
NM_024306.4:c.*887T= NP_077282.3:n.*887T=
XM_011523319.1:c.*887T= XP_011521621.1:n.*887T=
XM_011523319.2:c.*887T= XP_011521621.1:n.*887T=
NM_024306.5:c.*887T= MANE Select NP_077282.3:n.*887T=
Search 100 bp 5'
Search 100 bp 3'