Canonical Allele Identifier: CA431148993
Gene: ABCA12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215845345C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214980621C>G , CM000664.2:g.214980621C>G GRCh38
NC_000002.11:g.215845345C>G , CM000664.1:g.215845345C>G GRCh37
NC_000002.10:g.215553590C>G NCBI36
NG_007074.1:g.162807G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.4602G>C MANE Select ENSP00000272895.7:p.Thr1534=
ENST00000272895.11:c.4602G>C ENSP00000272895.7:p.Thr1534=
ENST00000389661.4:c.3648G>C ENSP00000374312.4:p.Thr1216=
NM_015657.3:c.3648G>C NP_056472.2:p.Thr1216=
NM_173076.2:c.4602G>C NP_775099.2:p.Thr1534=
NR_103740.1:n.4902G>C
XM_011510951.1:c.4611G>C XP_011509253.1:p.Thr1537=
XM_011510952.1:c.4611G>C XP_011509254.1:p.Thr1537=
XM_011510951.2:c.4611G>C XP_011509253.1:p.Thr1537=
NM_173076.3:c.4602G>C MANE Select NP_775099.2:p.Thr1534=
NR_103740.2:n.5100G>C
NM_015657.4:c.3648G>C NP_056472.2:p.Thr1216=