Canonical Allele Identifier: CA357237250

Gene: ALB

Linked Data

• dbSNP Id: rs1718796247
• MyVariant Identifiers: chr4:g.74274471T>C (hg19) ; chr4:g.73408754T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408754T>C , CM000666.2:g.73408754T>C	GRCh38
NC_000004.11:g.74274471T>C , CM000666.1:g.74274471T>C	GRCh37
NC_000004.10:g.74493335T>C	NCBI36
NG_009291.1:g.9500T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.431T>C MANE Select	ENSP00000295897.4:p.Val144Ala
ENST00000295897.8:c.431T>C	ENSP00000295897.4:p.Val144Ala
ENST00000401494.7:c.138-601T>C	ENSP00000384695.3:n.138-601T>C
ENST00000415165.6:c.138-3242T>C	ENSP00000401820.2:n.138-3242T>C
ENST00000441319.5:c.437T>C	ENSP00000392541.1:p.Val146Ala
ENST00000476441.6:c.80-601T>C	ENSP00000423727.1:n.80-601T>C
ENST00000503124.5:c.33-601T>C	ENSP00000421027.1:n.33-601T>C
ENST00000505649.5:n.117T>C
ENST00000509063.5:c.431T>C	ENSP00000422784.1:p.Val144Ala
ENST00000510166.5:n.467T>C
ENST00000514786.1:n.400T>C
ENST00000515133.5:n.472T>C
ENST00000621085.4:c.431T>C	ENSP00000483421.1:p.Val144Ala
ENST00000621628.4:c.431T>C	ENSP00000480485.1:p.Val144Ala
NM_000477.5:c.431T>C	NP_000468.1:p.Val144Ala
NM_000477.6:c.431T>C	NP_000468.1:p.Val144Ala
NM_000477.7:c.431T>C MANE Select	NP_000468.1:p.Val144Ala