Canonical Allele Identifier: CA64607838
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs975112539
gnomAD v4: 2-208124289-G-A
MyVariant Identifiers: chr2:g.208989013G>A (hg19) chr2:g.208124289G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124289G>A , CM000664.2:g.208124289G>A GRCh38
NC_000002.11:g.208989013G>A , CM000664.1:g.208989013G>A GRCh37
NC_000002.10:g.208697258G>A NCBI36
NG_008039.1:g.5301C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.75C>T MANE Select ENSP00000264376.4:p.Asn25=
ENST00000264376.4:c.75C>T ENSP00000264376.4:p.Asn25=
NM_006891.3:c.75C>T NP_008822.2:p.Asn25=
NR_038437.1:n.97+5064G>A
NM_006891.4:c.75C>T MANE Select NP_008822.2:p.Asn25=
Search 100 bp 5'
Search 100 bp 3'