Canonical Allele Identifier: CA164209531

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1039540610
• MyVariant Identifiers: chr7:g.107663845G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663845G>C , CM000669.2:g.107663845G>C	GRCh38
NC_000007.13:g.107304290G>C , CM000669.1:g.107304290G>C	GRCh37
NC_000007.12:g.107091526G>C	NCBI36
NG_008489.1:g.8211G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.304+410G>C MANE Select	ENSP00000494017.1:n.304+410G>C
ENST00000265715.7:c.304+410G>C	ENSP00000265715.3:n.304+410G>C
ENST00000440056.1:c.304+410G>C	ENSP00000394760.1:n.304+410G>C
NM_000441.1:c.304+410G>C	NP_000432.1:n.304+410G>C
XM_005250425.1:c.304+410G>C	XP_005250482.1:n.304+410G>C
XM_006716025.2:c.304+410G>C	XP_006716088.1:n.304+410G>C
XM_005250425.2:c.304+410G>C	XP_005250482.1:n.304+410G>C
XM_006716025.3:c.304+410G>C	XP_006716088.1:n.304+410G>C
XM_017012318.1:c.304+410G>C	XP_016867807.1:n.304+410G>C
NM_000441.2:c.304+410G>C MANE Select	NP_000432.1:n.304+410G>C