Canonical Allele Identifier: CA103381339
Gene:

Linked Data

dbSNP Id: rs538059088

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542964G>C , CM000666.2:g.105542964G>C GRCh38
NC_000004.11:g.106464121G>C , CM000666.1:g.106464121G>C GRCh37
NC_000004.10:g.106683570G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-255C>G
XR_939039.1:n.456-255C>G
XR_939040.1:n.296-1488C>G
XR_001741410.1:n.311-255C>G
XR_001741411.1:n.787-255C>G
XR_001741412.1:n.311-255C>G
XR_001741413.1:n.311-255C>G
XR_001741414.1:n.311-255C>G
XR_939038.2:n.311-255C>G
XR_939040.2:n.311-1488C>G