Canonical Allele Identifier: CA350092534
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208988877C>A (hg19) chr2:g.208124153C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124153C>A , CM000664.2:g.208124153C>A GRCh38
NC_000002.11:g.208988877C>A , CM000664.1:g.208988877C>A GRCh37
NC_000002.10:g.208697122C>A NCBI36
NG_008039.1:g.5437G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.211G>T MANE Select ENSP00000264376.4:p.Gly71Cys
ENST00000264376.4:c.211G>T ENSP00000264376.4:p.Gly71Cys
NM_006891.3:c.211G>T NP_008822.2:p.Gly71Cys
NR_038437.1:n.97+4928C>A
NM_006891.4:c.211G>T MANE Select NP_008822.2:p.Gly71Cys
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