Canonical Allele Identifier: CA350097684
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1695067556

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129683T>C , CM000664.2:g.208129683T>C GRCh38
NC_000002.11:g.208994407T>C , CM000664.1:g.208994407T>C GRCh37
NC_000002.10:g.208702652T>C NCBI36
NG_008038.1:g.5148A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10A>G MANE Select ENSP00000282141.3:p.Ile4Val
ENST00000282141.3:c.10A>G ENSP00000282141.3:p.Ile4Val
NM_020989.3:c.10A>G NP_066269.1:p.Ile4Val
NR_038437.1:n.98-7373T>C
XM_011510661.1:c.10A>G XP_011508963.1:p.Ile4Val
XM_011510662.1:c.10A>G XP_011508964.1:p.Ile4Val
XM_011510663.1:c.-120A>G XP_011508965.1:n.-120A>G
NM_020989.4:c.10A>G MANE Select NP_066269.1:p.Ile4Val