Canonical Allele Identifier: CA350093114
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs1251584271
gnomAD v2: 2-208989056-C-T
gnomAD v4: 2-208124332-C-T
MyVariant Identifiers: chr2:g.208989056C>T (hg19) chr2:g.208124332C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124332C>T , CM000664.2:g.208124332C>T GRCh38
NC_000002.11:g.208989056C>T , CM000664.1:g.208989056C>T GRCh37
NC_000002.10:g.208697301C>T NCBI36
NG_008039.1:g.5258G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.32G>A MANE Select ENSP00000264376.4:p.Gly11Asp
ENST00000264376.4:c.32G>A ENSP00000264376.4:p.Gly11Asp
NM_006891.3:c.32G>A NP_008822.2:p.Gly11Asp
NR_038437.1:n.97+5107C>T
NM_006891.4:c.32G>A MANE Select NP_008822.2:p.Gly11Asp
Search 100 bp 5'
Search 100 bp 3'