Canonical Allele Identifier: CA1327196939
Gene: ABCA12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064045A= , CM000664.2:g.215064045A= GRCh38
NC_000002.11:g.215928768A= , CM000664.1:g.215928768A= GRCh37
NC_000002.10:g.215637013A= NCBI36
NG_007074.1:g.79384T=

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.317+21T= MANE Select ENSP00000272895.7:n.317+21T=
ENST00000272895.11:c.317+21T= ENSP00000272895.7:n.317+21T=
NM_173076.2:c.317+21T= NP_775099.2:n.317+21T=
NR_103740.1:n.537+21T=
XM_011510951.1:c.317+21T= XP_011509253.1:n.317+21T=
XM_011510952.1:c.317+21T= XP_011509254.1:n.317+21T=
XM_011510951.2:c.317+21T= XP_011509253.1:n.317+21T=
NM_173076.3:c.317+21T= MANE Select NP_775099.2:n.317+21T=
NR_103740.2:n.735+21T=
Search 100 bp 5'
Search 100 bp 3'