Canonical Allele Identifier: CA350092523
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208988871T>C (hg19) chr2:g.208124147T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124147T>C , CM000664.2:g.208124147T>C GRCh38
NC_000002.11:g.208988871T>C , CM000664.1:g.208988871T>C GRCh37
NC_000002.10:g.208697116T>C NCBI36
NG_008039.1:g.5443A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.217A>G MANE Select ENSP00000264376.4:p.Ser73Gly
ENST00000264376.4:c.217A>G ENSP00000264376.4:p.Ser73Gly
NM_006891.3:c.217A>G NP_008822.2:p.Ser73Gly
NR_038437.1:n.97+4922T>C
NM_006891.4:c.217A>G MANE Select NP_008822.2:p.Ser73Gly
Search 100 bp 5'
Search 100 bp 3'