Canonical Allele Identifier: CA64823665

Gene: ABCA12

Linked Data

• dbSNP Id: rs113546371
• MyVariant Identifiers: chr2:g.215851184A>G (hg19) ; chr2:g.214986460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214986460A>G , CM000664.2:g.214986460A>G	GRCh38
NC_000002.11:g.215851184A>G , CM000664.1:g.215851184A>G	GRCh37
NC_000002.10:g.215559429A>G	NCBI36
NG_007074.1:g.156968T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4163+82T>C MANE Select	ENSP00000272895.7:n.4163+82T>C
ENST00000272895.11:c.4163+82T>C	ENSP00000272895.7:n.4163+82T>C
ENST00000389661.4:c.3209+82T>C	ENSP00000374312.4:n.3209+82T>C
NM_015657.3:c.3209+82T>C	NP_056472.2:n.3209+82T>C
NM_173076.2:c.4163+82T>C	NP_775099.2:n.4163+82T>C
NR_103740.1:n.4463+82T>C
XM_011510951.1:c.4172+82T>C	XP_011509253.1:n.4172+82T>C
XM_011510952.1:c.4172+82T>C	XP_011509254.1:n.4172+82T>C
XM_011510951.2:c.4172+82T>C	XP_011509253.1:n.4172+82T>C
NM_173076.3:c.4163+82T>C MANE Select	NP_775099.2:n.4163+82T>C
NR_103740.2:n.4661+82T>C
NM_015657.4:c.3209+82T>C	NP_056472.2:n.3209+82T>C