Canonical Allele Identifier: CA1327160941
Gene: ABCA12 HGNC NCBI

Linked Data

dbSNP Id: rs1699620226

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214980420T>C , CM000664.2:g.214980420T>C GRCh38
NC_000002.11:g.215845144T>C , CM000664.1:g.215845144T>C GRCh37
NC_000002.10:g.215553389T>C NCBI36
NG_007074.1:g.163008A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.4740+63A>G MANE Select ENSP00000272895.7:n.4740+63A>G
ENST00000272895.11:c.4740+63A>G ENSP00000272895.7:n.4740+63A>G
ENST00000389661.4:c.3786+63A>G ENSP00000374312.4:n.3786+63A>G
NM_015657.3:c.3786+63A>G NP_056472.2:n.3786+63A>G
NM_173076.2:c.4740+63A>G NP_775099.2:n.4740+63A>G
NR_103740.1:n.5040+63A>G
XM_011510951.1:c.4749+63A>G XP_011509253.1:n.4749+63A>G
XM_011510952.1:c.4749+63A>G XP_011509254.1:n.4749+63A>G
XM_011510951.2:c.4749+63A>G XP_011509253.1:n.4749+63A>G
NM_173076.3:c.4740+63A>G MANE Select NP_775099.2:n.4740+63A>G
NR_103740.2:n.5238+63A>G
NM_015657.4:c.3786+63A>G NP_056472.2:n.3786+63A>G