Canonical Allele Identifier: CA350461284

Gene: ABCA12

Linked Data

• dbSNP Id: rs1201529935
• gnomAD v2: 2-215845362-T-C
• gnomAD v4: 2-214980638-T-C
• MyVariant Identifiers: chr2:g.215845362T>C (hg19) ; chr2:g.214980638T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980638T>C , CM000664.2:g.214980638T>C	GRCh38
NC_000002.11:g.215845362T>C , CM000664.1:g.215845362T>C	GRCh37
NC_000002.10:g.215553607T>C	NCBI36
NG_007074.1:g.162790A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4585A>G MANE Select	ENSP00000272895.7:p.Thr1529Ala
ENST00000272895.11:c.4585A>G	ENSP00000272895.7:p.Thr1529Ala
ENST00000389661.4:c.3631A>G	ENSP00000374312.4:p.Thr1211Ala
NM_015657.3:c.3631A>G	NP_056472.2:p.Thr1211Ala
NM_173076.2:c.4585A>G	NP_775099.2:p.Thr1529Ala
NR_103740.1:n.4885A>G
XM_011510951.1:c.4594A>G	XP_011509253.1:p.Thr1532Ala
XM_011510952.1:c.4594A>G	XP_011509254.1:p.Thr1532Ala
XM_011510951.2:c.4594A>G	XP_011509253.1:p.Thr1532Ala
NM_173076.3:c.4585A>G MANE Select	NP_775099.2:p.Thr1529Ala
NR_103740.2:n.5083A>G
NM_015657.4:c.3631A>G	NP_056472.2:p.Thr1211Ala