Canonical Allele Identifier: CA2662869357
Gene: CRYGC HGNC NCBI

Linked Data

gnomAD v4: 2-208129897-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129897G>T , CM000664.2:g.208129897G>T GRCh38
NC_000002.11:g.208994621G>T , CM000664.1:g.208994621G>T GRCh37
NC_000002.10:g.208702866G>T NCBI36
NG_008038.1:g.4934C>A

Transcript Alleles

HGVS Amino-acid Change
NR_038437.1:n.98-7159G>T
XM_011510661.1:c.-79-26C>A XP_011508963.1:n.-79-26C>A
XM_011510662.1:c.-79-26C>A XP_011508964.1:n.-79-26C>A
XM_011510663.1:c.-120-214C>A XP_011508965.1:n.-120-214C>A
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