Canonical Allele Identifier: CA1327140918
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

dbSNP Id: rs1698088590
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214932455T>C , CM000664.2:g.214932455T>C GRCh38
NC_000002.11:g.215797179T>C , CM000664.1:g.215797179T>C GRCh37
NC_000002.10:g.215505424T>C NCBI36
NG_007074.1:g.210973A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.*179A>G (ABCA12) MANE Select ENSP00000272895.7:n.*179A>G
ENST00000272895.11:c.*179A>G (ABCA12) ENSP00000272895.7:n.*179A>G
NM_015657.3:c.*179A>G (ABCA12) NP_056472.2:n.*179A>G
NM_173076.2:c.*179A>G (ABCA12) NP_775099.2:n.*179A>G
NR_103740.1:n.8267A>G (ABCA12)
NR_110292.1:n.322-15370T>C (SNHG31)
XM_011510951.1:c.*179A>G (ABCA12) XP_011509253.1:n.*179A>G
XM_011510951.2:c.*179A>G (ABCA12) XP_011509253.1:n.*179A>G
NM_173076.3:c.*179A>G (ABCA12) MANE Select NP_775099.2:n.*179A>G
NR_103740.2:n.8465A>G (ABCA12)
NM_015657.4:c.*179A>G (ABCA12) NP_056472.2:n.*179A>G
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