Canonical Allele Identifier: CA2662974092
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

gnomAD v4: 2-214932573-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214932573T>C , CM000664.2:g.214932573T>C GRCh38
NC_000002.11:g.215797297T>C , CM000664.1:g.215797297T>C GRCh37
NC_000002.10:g.215505542T>C NCBI36
NG_007074.1:g.210855A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.*61A>G (ABCA12) MANE Select ENSP00000272895.7:n.*61A>G
ENST00000272895.11:c.*61A>G (ABCA12) ENSP00000272895.7:n.*61A>G
NM_015657.3:c.*61A>G (ABCA12) NP_056472.2:n.*61A>G
NM_173076.2:c.*61A>G (ABCA12) NP_775099.2:n.*61A>G
NR_103740.1:n.8149A>G (ABCA12)
NR_110292.1:n.322-15252T>C (SNHG31)
XM_011510951.1:c.*61A>G (ABCA12) XP_011509253.1:n.*61A>G
XM_011510951.2:c.*61A>G (ABCA12) XP_011509253.1:n.*61A>G
NM_173076.3:c.*61A>G (ABCA12) MANE Select NP_775099.2:n.*61A>G
NR_103740.2:n.8347A>G (ABCA12)
NM_015657.4:c.*61A>G (ABCA12) NP_056472.2:n.*61A>G
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