Canonical Allele Identifier: CA1041738581
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1004216287

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129890C>A , CM000664.2:g.208129890C>A GRCh38
NC_000002.11:g.208994614C>A , CM000664.1:g.208994614C>A GRCh37
NC_000002.10:g.208702859C>A NCBI36
NG_008038.1:g.4941G>T

Transcript Alleles

HGVS Amino-acid Change
NR_038437.1:n.98-7166C>A
XM_011510661.1:c.-79-19G>T XP_011508963.1:n.-79-19G>T
XM_011510662.1:c.-79-19G>T XP_011508964.1:n.-79-19G>T
XM_011510663.1:c.-120-207G>T XP_011508965.1:n.-120-207G>T