Canonical Allele Identifier: CA350097545
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1231313637

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129647T>C , CM000664.2:g.208129647T>C GRCh38
NC_000002.11:g.208994371T>C , CM000664.1:g.208994371T>C GRCh37
NC_000002.10:g.208702616T>C NCBI36
NG_008038.1:g.5184A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.46A>G MANE Select ENSP00000282141.3:p.Ser16Gly
ENST00000282141.3:c.46A>G ENSP00000282141.3:p.Ser16Gly
NM_020989.3:c.46A>G NP_066269.1:p.Ser16Gly
NR_038437.1:n.98-7409T>C
XM_011510661.1:c.46A>G XP_011508963.1:p.Ser16Gly
XM_011510662.1:c.46A>G XP_011508964.1:p.Ser16Gly
XM_011510663.1:c.-84A>G XP_011508965.1:n.-84A>G
NM_020989.4:c.46A>G MANE Select NP_066269.1:p.Ser16Gly