Canonical Allele Identifier: CA430964612
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208988914C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124190C>A , CM000664.2:g.208124190C>A GRCh38
NC_000002.11:g.208988914C>A , CM000664.1:g.208988914C>A GRCh37
NC_000002.10:g.208697159C>A NCBI36
NG_008039.1:g.5400G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264376.5:c.174G>T MANE Select ENSP00000264376.4:p.Leu58=
ENST00000264376.4:c.174G>T ENSP00000264376.4:p.Leu58=
NM_006891.3:c.174G>T NP_008822.2:p.Leu58=
NR_038437.1:n.97+4965C>A
NM_006891.4:c.174G>T MANE Select NP_008822.2:p.Leu58=
Search 100 bp 5'
Search 100 bp 3'