Canonical Allele Identifier: CA350096622
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1574551151
MyVariant Identifiers: chr2:g.208994230A>C (hg19) chr2:g.208129506A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129506A>C , CM000664.2:g.208129506A>C GRCh38
NC_000002.11:g.208994230A>C , CM000664.1:g.208994230A>C GRCh37
NC_000002.10:g.208702475A>C NCBI36
NG_008038.1:g.5325T>G
NG_008039.1:g.84T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.187T>G MANE Select ENSP00000282141.3:p.Tyr63Asp
ENST00000282141.3:c.187T>G ENSP00000282141.3:p.Tyr63Asp
NM_020989.3:c.187T>G NP_066269.1:p.Tyr63Asp
NR_038437.1:n.98-7550A>C
XM_011510661.1:c.187T>G XP_011508963.1:p.Tyr63Asp
XM_011510662.1:c.187T>G XP_011508964.1:p.Tyr63Asp
XM_011510663.1:c.58T>G XP_011508965.1:p.Tyr20Asp
NM_020989.4:c.187T>G MANE Select NP_066269.1:p.Tyr63Asp
Search 100 bp 5'
Search 100 bp 3'