Canonical Allele Identifier: CA1327174255

Gene: ABCA12

Linked Data

• dbSNP Id: rs1700380650

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011813A>C , CM000664.2:g.215011813A>C	GRCh38
NC_000002.11:g.215876537A>C , CM000664.1:g.215876537A>C	GRCh37
NC_000002.10:g.215584782A>C	NCBI36
NG_007074.1:g.131615T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2121+158T>G MANE Select	ENSP00000272895.7:n.2121+158T>G
ENST00000272895.11:c.2121+158T>G	ENSP00000272895.7:n.2121+158T>G
ENST00000389661.4:c.1167+158T>G	ENSP00000374312.4:n.1167+158T>G
NM_015657.3:c.1167+158T>G	NP_056472.2:n.1167+158T>G
NM_173076.2:c.2121+158T>G	NP_775099.2:n.2121+158T>G
NR_103740.1:n.2365+158T>G
XM_011510951.1:c.2121+158T>G	XP_011509253.1:n.2121+158T>G
XM_011510952.1:c.2121+158T>G	XP_011509254.1:n.2121+158T>G
XM_011510951.2:c.2121+158T>G	XP_011509253.1:n.2121+158T>G
NM_173076.3:c.2121+158T>G MANE Select	NP_775099.2:n.2121+158T>G
NR_103740.2:n.2563+158T>G
NM_015657.4:c.1167+158T>G	NP_056472.2:n.1167+158T>G