Canonical Allele Identifier: CA1323928793
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs1694923452
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124010T>A , CM000664.2:g.208124010T>A GRCh38
NC_000002.11:g.208988734T>A , CM000664.1:g.208988734T>A GRCh37
NC_000002.10:g.208696979T>A NCBI36
NG_008039.1:g.5580A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+102A>T MANE Select ENSP00000264376.4:n.252+102A>T
ENST00000264376.4:c.252+102A>T ENSP00000264376.4:n.252+102A>T
NM_006891.3:c.252+102A>T NP_008822.2:n.252+102A>T
NR_038437.1:n.97+4785T>A
NM_006891.4:c.252+102A>T MANE Select NP_008822.2:n.252+102A>T
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