Canonical Allele Identifier: CA1327174207

Gene: ABCA12

Linked Data

• dbSNP Id: rs1700378222
• gnomAD v4: 2-215011702-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011702C>T , CM000664.2:g.215011702C>T	GRCh38
NC_000002.11:g.215876426C>T , CM000664.1:g.215876426C>T	GRCh37
NC_000002.10:g.215584671C>T	NCBI36
NG_007074.1:g.131726G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.2122-53G>A MANE Select	ENSP00000272895.7:n.2122-53G>A
ENST00000272895.11:c.2122-53G>A	ENSP00000272895.7:n.2122-53G>A
ENST00000389661.4:c.1168-53G>A	ENSP00000374312.4:n.1168-53G>A
NM_015657.3:c.1168-53G>A	NP_056472.2:n.1168-53G>A
NM_173076.2:c.2122-53G>A	NP_775099.2:n.2122-53G>A
NR_103740.1:n.2366-53G>A
XM_011510951.1:c.2122-53G>A	XP_011509253.1:n.2122-53G>A
XM_011510952.1:c.2122-53G>A	XP_011509254.1:n.2122-53G>A
XM_011510951.2:c.2122-53G>A	XP_011509253.1:n.2122-53G>A
NM_173076.3:c.2122-53G>A MANE Select	NP_775099.2:n.2122-53G>A
NR_103740.2:n.2564-53G>A
NM_015657.4:c.1168-53G>A	NP_056472.2:n.1168-53G>A