Canonical Allele Identifier: CA1397901620
Gene: CSTA HGNC NCBI

Linked Data

dbSNP Id: rs2075193000
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122329712C>T , CM000665.2:g.122329712C>T GRCh38
NC_000003.11:g.122048559C>T , CM000665.1:g.122048559C>T GRCh37
NC_000003.10:g.123531249C>T NCBI36
NG_027995.1:g.9549C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264474.4:c.66+4354C>T MANE Select ENSP00000264474.3:n.66+4354C>T
ENST00000264474.3:c.66+4354C>T ENSP00000264474.3:n.66+4354C>T
ENST00000479204.1:c.66+4354C>T ENSP00000418891.1:n.66+4354C>T
NM_005213.3:c.66+4354C>T NP_005204.1:n.66+4354C>T
NM_005213.4:c.66+4354C>T MANE Select NP_005204.1:n.66+4354C>T
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