Canonical Allele Identifier: CA2092615
Gene: ABCA12 HGNC NCBI

Linked Data

dbSNP Id: rs757915875

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064118G>C , CM000664.2:g.215064118G>C GRCh38
NC_000002.11:g.215928841G>C , CM000664.1:g.215928841G>C GRCh37
NC_000002.10:g.215637086G>C NCBI36
NG_007074.1:g.79311C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.265C>G MANE Select ENSP00000272895.7:p.Pro89Ala
ENST00000272895.11:c.265C>G ENSP00000272895.7:p.Pro89Ala
NM_173076.2:c.265C>G NP_775099.2:p.Pro89Ala
NR_103740.1:n.485C>G
XM_011510951.1:c.265C>G XP_011509253.1:p.Pro89Ala
XM_011510952.1:c.265C>G XP_011509254.1:p.Pro89Ala
XM_011510951.2:c.265C>G XP_011509253.1:p.Pro89Ala
NM_173076.3:c.265C>G MANE Select NP_775099.2:p.Pro89Ala
NR_103740.2:n.683C>G