Canonical Allele Identifier: CA350483734
Gene: ABCA12 HGNC NCBI

Linked Data

dbSNP Id: rs1559144924

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215011600G>C , CM000664.2:g.215011600G>C GRCh38
NC_000002.11:g.215876324G>C , CM000664.1:g.215876324G>C GRCh37
NC_000002.10:g.215584569G>C NCBI36
NG_007074.1:g.131828C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.2171C>G MANE Select ENSP00000272895.7:p.Thr724Ser
ENST00000272895.11:c.2171C>G ENSP00000272895.7:p.Thr724Ser
ENST00000389661.4:c.1217C>G ENSP00000374312.4:p.Thr406Ser
NM_015657.3:c.1217C>G NP_056472.2:p.Thr406Ser
NM_173076.2:c.2171C>G NP_775099.2:p.Thr724Ser
NR_103740.1:n.2415C>G
XM_011510951.1:c.2171C>G XP_011509253.1:p.Thr724Ser
XM_011510952.1:c.2171C>G XP_011509254.1:p.Thr724Ser
XM_011510951.2:c.2171C>G XP_011509253.1:p.Thr724Ser
NM_173076.3:c.2171C>G MANE Select NP_775099.2:p.Thr724Ser
NR_103740.2:n.2613C>G
NM_015657.4:c.1217C>G NP_056472.2:p.Thr406Ser