Canonical Allele Identifier: CA350092536
Gene: CRYGD HGNC NCBI

Linked Data

gnomAD v4: 2-208124153-C-G
MyVariant Identifiers: chr2:g.208988877C>G (hg19) chr2:g.208124153C>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.211G>C MANE Select ENSP00000264376.4:p.Gly71Arg
ENST00000264376.4:c.211G>C ENSP00000264376.4:p.Gly71Arg
NM_006891.3:c.211G>C NP_008822.2:p.Gly71Arg
NR_038437.1:n.97+4928C>G
NM_006891.4:c.211G>C MANE Select NP_008822.2:p.Gly71Arg
Search 100 bp 5'
Search 100 bp 3'