Canonical Allele Identifier: CA431388387

Gene: ABCA12

Linked Data

• dbSNP Id: rs1269691889
• gnomAD v2: 2-215855687-A-G
• MyVariant Identifiers: chr2:g.215855687A>G (hg19) ; chr2:g.214990963A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214990963A>G , CM000664.2:g.214990963A>G	GRCh38
NC_000002.11:g.215855687A>G , CM000664.1:g.215855687A>G	GRCh37
NC_000002.10:g.215563932A>G	NCBI36
NG_007074.1:g.152465T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.3363T>C MANE Select	ENSP00000272895.7:p.Phe1121=
ENST00000272895.11:c.3363T>C	ENSP00000272895.7:p.Phe1121=
ENST00000389661.4:c.2409T>C	ENSP00000374312.4:p.Phe803=
NM_015657.3:c.2409T>C	NP_056472.2:p.Phe803=
NM_173076.2:c.3363T>C	NP_775099.2:p.Phe1121=
NR_103740.1:n.3663T>C
XM_011510951.1:c.3363T>C	XP_011509253.1:p.Phe1121=
XM_011510952.1:c.3363T>C	XP_011509254.1:p.Phe1121=
XM_011510951.2:c.3363T>C	XP_011509253.1:p.Phe1121=
NM_173076.3:c.3363T>C MANE Select	NP_775099.2:p.Phe1121=
NR_103740.2:n.3861T>C
NM_015657.4:c.2409T>C	NP_056472.2:p.Phe803=