Canonical Allele Identifier: CA2092252

Gene: ABCA12

Linked Data

• dbSNP Id: rs149243979
• ExAC: 2:215884512 T / A
• gnomAD v2: 2-215884512-T-A
• gnomAD v3: 2-215019788-T-A
• gnomAD v4: 2-215019788-T-A
• MyVariant Identifiers: chr2:g.215884512T>A (hg19) ; chr2:g.215019788T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215019788T>A , CM000664.2:g.215019788T>A	GRCh38
NC_000002.11:g.215884512T>A , CM000664.1:g.215884512T>A	GRCh37
NC_000002.10:g.215592757T>A	NCBI36
NG_007074.1:g.123640A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.1296A>T MANE Select	ENSP00000272895.7:p.Gln432His
ENST00000272895.11:c.1296A>T	ENSP00000272895.7:p.Gln432His
ENST00000389661.4:c.342A>T	ENSP00000374312.4:p.Gln114His
NM_015657.3:c.342A>T	NP_056472.2:p.Gln114His
NM_173076.2:c.1296A>T	NP_775099.2:p.Gln432His
NR_103740.1:n.1540A>T
XM_011510951.1:c.1296A>T	XP_011509253.1:p.Gln432His
XM_011510952.1:c.1296A>T	XP_011509254.1:p.Gln432His
XM_011510951.2:c.1296A>T	XP_011509253.1:p.Gln432His
NM_173076.3:c.1296A>T MANE Select	NP_775099.2:p.Gln432His
NR_103740.2:n.1738A>T
NM_015657.4:c.342A>T	NP_056472.2:p.Gln114His