Canonical Allele Identifier: CA1327196931
Gene: ABCA12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064028T= , CM000664.2:g.215064028T= GRCh38
NC_000002.11:g.215928751T= , CM000664.1:g.215928751T= GRCh37
NC_000002.10:g.215636996T= NCBI36
NG_007074.1:g.79401A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.317+38A= MANE Select ENSP00000272895.7:n.317+38A=
ENST00000272895.11:c.317+38A= ENSP00000272895.7:n.317+38A=
NM_173076.2:c.317+38A= NP_775099.2:n.317+38A=
NR_103740.1:n.537+38A=
XM_011510951.1:c.317+38A= XP_011509253.1:n.317+38A=
XM_011510952.1:c.317+38A= XP_011509254.1:n.317+38A=
XM_011510951.2:c.317+38A= XP_011509253.1:n.317+38A=
NM_173076.3:c.317+38A= MANE Select NP_775099.2:n.317+38A=
NR_103740.2:n.735+38A=
Search 100 bp 5'
Search 100 bp 3'