Canonical Allele Identifier: CA64814895

Gene: ABCA12

Linked Data

• ClinVar Variation Id: 721244
• ClinVar RCV Id: RCV000894717
• dbSNP Id: rs966377695
• gnomAD v2: 2-215845306-G-A
• gnomAD v3: 2-214980582-G-A
• gnomAD v4: 2-214980582-G-A
• COSMIC: COSM3577452 ; COSM4897499
• MyVariant Identifiers: chr2:g.215845306G>A (hg19) ; chr2:g.214980582G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980582G>A , CM000664.2:g.214980582G>A	GRCh38
NC_000002.11:g.215845306G>A , CM000664.1:g.215845306G>A	GRCh37
NC_000002.10:g.215553551G>A	NCBI36
NG_007074.1:g.162846C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4641C>T MANE Select	ENSP00000272895.7:p.Ile1547=
ENST00000272895.11:c.4641C>T	ENSP00000272895.7:p.Ile1547=
ENST00000389661.4:c.3687C>T	ENSP00000374312.4:p.Ile1229=
NM_015657.3:c.3687C>T	NP_056472.2:p.Ile1229=
NM_173076.2:c.4641C>T	NP_775099.2:p.Ile1547=
NR_103740.1:n.4941C>T
XM_011510951.1:c.4650C>T	XP_011509253.1:p.Ile1550=
XM_011510952.1:c.4650C>T	XP_011509254.1:p.Ile1550=
XM_011510951.2:c.4650C>T	XP_011509253.1:p.Ile1550=
NM_173076.3:c.4641C>T MANE Select	NP_775099.2:p.Ile1547=
NR_103740.2:n.5139C>T
NM_015657.4:c.3687C>T	NP_056472.2:p.Ile1229=