Canonical Allele Identifier: CA2662973835

Gene: ABCA12 SNHG31

Linked Data

• gnomAD v4: 2-214932127-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932127T>C , CM000664.2:g.214932127T>C	GRCh38
NC_000002.11:g.215796851T>C , CM000664.1:g.215796851T>C	GRCh37
NC_000002.10:g.215505096T>C	NCBI36
NG_007074.1:g.211301A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*507A>G (ABCA12) MANE Select	ENSP00000272895.7:n.*507A>G
ENST00000272895.11:c.*507A>G (ABCA12)	ENSP00000272895.7:n.*507A>G
NM_015657.3:c.*507A>G (ABCA12)	NP_056472.2:n.*507A>G
NM_173076.2:c.*507A>G (ABCA12)	NP_775099.2:n.*507A>G
NR_103740.1:n.8595A>G (ABCA12)
NR_110292.1:n.322-15698T>C (SNHG31)
XM_011510951.1:c.*507A>G (ABCA12)	XP_011509253.1:n.*507A>G
XM_011510951.2:c.*507A>G (ABCA12)	XP_011509253.1:n.*507A>G
NM_173076.3:c.*507A>G (ABCA12) MANE Select	NP_775099.2:n.*507A>G
NR_103740.2:n.8793A>G (ABCA12)
NM_015657.4:c.*507A>G (ABCA12)	NP_056472.2:n.*507A>G