Canonical Allele Identifier: CA431116235
Gene: CRYGC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208994405G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129681G>A , CM000664.2:g.208129681G>A GRCh38
NC_000002.11:g.208994405G>A , CM000664.1:g.208994405G>A GRCh37
NC_000002.10:g.208702650G>A NCBI36
NG_008038.1:g.5150C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.12C>T MANE Select ENSP00000282141.3:p.Ile4=
ENST00000282141.3:c.12C>T ENSP00000282141.3:p.Ile4=
NM_020989.3:c.12C>T NP_066269.1:p.Ile4=
NR_038437.1:n.98-7375G>A
XM_011510661.1:c.12C>T XP_011508963.1:p.Ile4=
XM_011510662.1:c.12C>T XP_011508964.1:p.Ile4=
XM_011510663.1:c.-118C>T XP_011508965.1:n.-118C>T
NM_020989.4:c.12C>T MANE Select NP_066269.1:p.Ile4=