Canonical Allele Identifier: CA350097347
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129590A>C , CM000664.2:g.208129590A>C GRCh38
NC_000002.11:g.208994314A>C , CM000664.1:g.208994314A>C GRCh37
NC_000002.10:g.208702559A>C NCBI36
NG_008038.1:g.5241T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.103T>G MANE Select ENSP00000282141.3:p.Ser35Ala
ENST00000282141.3:c.103T>G ENSP00000282141.3:p.Ser35Ala
NM_020989.3:c.103T>G NP_066269.1:p.Ser35Ala
NR_038437.1:n.98-7466A>C
XM_011510661.1:c.103T>G XP_011508963.1:p.Ser35Ala
XM_011510662.1:c.103T>G XP_011508964.1:p.Ser35Ala
XM_011510663.1:c.-27T>G XP_011508965.1:n.-27T>G
NM_020989.4:c.103T>G MANE Select NP_066269.1:p.Ser35Ala