Canonical Allele Identifier: CA236762907

Gene: FAM186A

Linked Data

• dbSNP Id: rs958420363
• MyVariant Identifiers: chr12:g.50754472A>T (hg19) ; chr12:g.50360689A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50360689A>T , CM000674.2:g.50360689A>T	GRCh38
NC_000012.11:g.50754472A>T , CM000674.1:g.50754472A>T	GRCh37
NC_000012.10:g.49040739A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327337.6:c.583+67T>A MANE Select	ENSP00000329995.5:n.583+67T>A
ENST00000327337.5:c.583+67T>A	ENSP00000329995.5:n.583+67T>A
ENST00000543111.5:c.583+67T>A	ENSP00000441337.1:n.583+67T>A
NM_001145475.1:c.583+67T>A	NP_001138947.1:n.583+67T>A
XM_006719231.2:c.583+67T>A	XP_006719294.1:n.583+67T>A
XM_011537890.1:c.583+67T>A	XP_011536192.1:n.583+67T>A
XM_011537891.1:c.412+2456T>A	XP_011536193.1:n.412+2456T>A
XM_011537892.1:c.154+67T>A	XP_011536194.1:n.154+67T>A
NM_001145475.2:c.583+67T>A	NP_001138947.1:n.583+67T>A
XM_006719231.3:c.583+67T>A	XP_006719294.1:n.583+67T>A
XM_011537890.2:c.583+67T>A	XP_011536192.1:n.583+67T>A
NM_001145475.3:c.583+67T>A MANE Select	NP_001138947.1:n.583+67T>A