Canonical Allele Identifier: CA15207645

Gene: FSHR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48950462C>T , CM000664.2:g.48950462C>T	GRCh38
NC_000002.11:g.49177601C>T , CM000664.1:g.49177601C>T	GRCh37
NC_000002.10:g.49031105C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011532737.1:c.957-5553G>A	XP_011531039.1:n.957-5553G>A
XM_011532738.1:c.956+18236G>A	XP_011531040.1:n.956+18236G>A
XM_011532739.1:c.956+18236G>A	XP_011531041.1:n.956+18236G>A