Canonical Allele Identifier: CA15520286
Gene: AHCYL2 HGNC NCBI

Linked Data

dbSNP Id: rs11979476

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129353915T>G , CM000669.2:g.129353915T>G GRCh38
NC_000007.13:g.128993756T>G , CM000669.1:g.128993756T>G GRCh37
NC_000007.12:g.128780992T>G NCBI36
NG_029180.1:g.133902T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325006.8:c.364-25723T>G MANE Select ENSP00000315931.3:n.364-25723T>G
ENST00000325006.7:c.364-25723T>G ENSP00000315931.3:n.364-25723T>G
ENST00000446544.6:c.364-25726T>G ENSP00000413639.2:n.364-25726T>G
ENST00000461161.5:n.159+2254T>G
NM_001130720.2:c.364-25726T>G NP_001124192.1:n.364-25726T>G
NM_015328.3:c.364-25723T>G NP_056143.1:n.364-25723T>G
XM_017011904.1:c.-255-25726T>G XP_016867393.1:n.-255-25726T>G
XM_017011906.1:c.-258-25723T>G XP_016867395.1:n.-258-25723T>G
NM_001130720.3:c.364-25726T>G NP_001124192.1:n.364-25726T>G
NM_015328.4:c.364-25723T>G MANE Select NP_056143.1:n.364-25723T>G
NM_001393387.1:c.364-25723T>G NP_001380316.1:n.364-25723T>G
NR_171671.1:n.411-23627T>G