Canonical Allele Identifier: CA12704271
Gene: AHCYL2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11766298

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129365006C>T , CM000669.2:g.129365006C>T GRCh38
NC_000007.13:g.129004847C>T , CM000669.1:g.129004847C>T GRCh37
NC_000007.12:g.128792083C>T NCBI36
NG_029180.1:g.144993C>T

Transcript Alleles

HGVS Amino-acid change
NM_001130720.2:c.364-14635C>T VV NP_001124192.1:p.=
NM_015328.3:c.364-14632C>T VV NP_056143.1:p.=
XR_927961.1:n.86-1533G>A
XM_017011904.1:c.-255-14635C>T XP_016867393.1:p.=
XM_017011906.1:c.-258-14632C>T XP_016867395.1:p.=
ENST00000325006.7:c.364-14632C>T ENSP00000315931.3:p.=
ENST00000446544.6:c.364-14635C>T ENSP00000413639.2:p.=
ENST00000461161.5:n.159+13345C>T