Canonical Allele Identifier: CA2662976193
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

gnomAD v4: 2-214953822-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214953822G>T , CM000664.2:g.214953822G>T GRCh38
NC_000002.11:g.215818546G>T , CM000664.1:g.215818546G>T GRCh37
NC_000002.10:g.215526791G>T NCBI36
NG_007074.1:g.189606C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.6647+32C>A (ABCA12) MANE Select ENSP00000272895.7:n.6647+32C>A
ENST00000272895.11:c.6647+32C>A (ABCA12) ENSP00000272895.7:n.6647+32C>A
ENST00000389661.4:c.5693+32C>A (ABCA12) ENSP00000374312.4:n.5693+32C>A
NM_015657.3:c.5693+32C>A (ABCA12) NP_056472.2:n.5693+32C>A
NM_173076.2:c.6647+32C>A (ABCA12) NP_775099.2:n.6647+32C>A
NR_103740.1:n.6947+32C>A (ABCA12)
NR_110292.1:n.444+5875G>T (SNHG31)
XM_011510951.1:c.6656+32C>A (ABCA12) XP_011509253.1:n.6656+32C>A
XM_011510951.2:c.6656+32C>A (ABCA12) XP_011509253.1:n.6656+32C>A
NM_173076.3:c.6647+32C>A (ABCA12) MANE Select NP_775099.2:n.6647+32C>A
NR_103740.2:n.7145+32C>A (ABCA12)
NM_015657.4:c.5693+32C>A (ABCA12) NP_056472.2:n.5693+32C>A
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