Canonical Allele Identifier: CA350097019
Gene: CRYGC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208994264G>C (hg19) chr2:g.208129540G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129540G>C , CM000664.2:g.208129540G>C GRCh38
NC_000002.11:g.208994264G>C , CM000664.1:g.208994264G>C GRCh37
NC_000002.10:g.208702509G>C NCBI36
NG_008038.1:g.5291C>G
NG_008039.1:g.50C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.153C>G MANE Select ENSP00000282141.3:p.Tyr51Ter
ENST00000282141.3:c.153C>G ENSP00000282141.3:p.Tyr51Ter
NM_020989.3:c.153C>G NP_066269.1:p.Tyr51Ter
NR_038437.1:n.98-7516G>C
XM_011510661.1:c.153C>G XP_011508963.1:p.Tyr51Ter
XM_011510662.1:c.153C>G XP_011508964.1:p.Tyr51Ter
XM_011510663.1:c.24C>G XP_011508965.1:p.Tyr8Ter
NM_020989.4:c.153C>G MANE Select NP_066269.1:p.Tyr51Ter
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