Canonical Allele Identifier: CA1929213270
Gene:

Linked Data

dbSNP Id: rs1848181559

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762441T>C , CM000672.2:g.94762441T>C GRCh38
NC_000010.10:g.96522198T>C , CM000672.1:g.96522198T>C GRCh37
NC_000010.9:g.96512188T>C NCBI36
NG_008384.2:g.4736T>C
NG_008384.3:g.4761T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12617T>C ENSP00000483243.1:n.932-12617T>C