Canonical Allele Identifier: CA127350
Gene: GYPC HGNC NCBI

Linked Data

ClinVar Variation Id: 17726
ClinVar RCV Id: RCV000019300
dbSNP Id: rs121912760

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.126656286A>G , CM000664.2:g.126656286A>G GRCh38
NC_000002.11:g.127413862A>G , CM000664.1:g.127413862A>G GRCh37
NC_000002.10:g.127130332A>G NCBI36
NG_007479.1:g.5179A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259254.9:c.23A>G MANE Select ENSP00000259254.4:p.Asn8Ser
ENST00000356887.12:c.-859A>G ENSP00000349354.7:n.-859A>G
ENST00000484700.2:n.154A>G
ENST00000259254.8:c.23A>G ENSP00000259254.4:p.Asn8Ser
ENST00000356887.11:c.-859A>G ENSP00000349354.7:n.-859A>G
ENST00000409836.3:c.23A>G ENSP00000386904.3:p.Asn8Ser
ENST00000459787.1:n.145A>G
ENST00000464053.1:n.98A>G
ENST00000484700.1:n.154A>G
NM_001256584.1:c.-859A>G NP_001243513.1:n.-859A>G
NM_002101.4:c.23A>G NP_002092.1:p.Asn8Ser
NM_016815.3:c.23A>G NP_058131.1:p.Asn8Ser
NM_002101.5:c.23A>G MANE Select NP_002092.1:p.Asn8Ser
NM_001256584.2:c.-859A>G NP_001243513.1:n.-859A>G
NM_016815.4:c.23A>G NP_058131.1:p.Asn8Ser