Canonical Allele Identifier: CA350092531
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208988876C>A (hg19) chr2:g.208124152C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124152C>A , CM000664.2:g.208124152C>A GRCh38
NC_000002.11:g.208988876C>A , CM000664.1:g.208988876C>A GRCh37
NC_000002.10:g.208697121C>A NCBI36
NG_008039.1:g.5438G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.212G>T MANE Select ENSP00000264376.4:p.Gly71Val
ENST00000264376.4:c.212G>T ENSP00000264376.4:p.Gly71Val
NM_006891.3:c.212G>T NP_008822.2:p.Gly71Val
NR_038437.1:n.97+4927C>A
NM_006891.4:c.212G>T MANE Select NP_008822.2:p.Gly71Val
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